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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396872Generated: October 25, 2026

1-Methylimidazole → Phenylmethyl (3S)-3-{[(6-chloro-2-pyridinyl)amino]carbonyl}-2-[(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl]-1-pyrazolidinecarboxylate

https://huagongshe.com/reaction/1396872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Amino-6-chloropyridineHCID 206246—
Reactant2-[(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl]-1-{[(phenylmethyl)oxy]carbonyl}-3-pyrazolidinecarboxylic acidHCID 86706341—
SolventDichloromethaneHCID 6344—
Solvent(3S)-2-[(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl]-1-{[(phenylmethyl)oxy]carbonyl}-3-pyrazolidinecarboxylic acidHCID 86706346—
ProductPhenylmethyl (3S)-3-{[(6-chloro-2-pyridinyl)amino]carbonyl}-2-[(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl]-1-pyrazolidinecarboxylateHCID 8670634774%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-[(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl]-1-{[(phenylmethyl)oxy]carbonyl}-3-pyrazolidine carboxylic acid (as a mixture of diastereomers enriched in (3S)-2-[(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl]-1-{[(phenylmethyl)oxy]carbonyl}-3-pyrazolidinecarboxylic acid) (300 mg, 0.558 mmol) in dichloromethane (5 ml) was added 1-methylimidazole (133 μl, 1.674 mmol) and cooled to 0° C. Mesyl chloride (56 μL, 0.725 mmol) was added dropwise at 0° C. and stirred for 1 hr at rt. The mixture was then treated with 2-amino-6-chloropyridine (86 mg, 0.67 mmol). The solvent mixture was removed. The residue was diluted with MeOH and purified by reverse-phase HPLC to afford 268 mg (0.413 mmol, 74%) of the title compound. LC/MS: (M+H)+: 648.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-b9f4b97b6fe44fa2b9aa5606260cc5d4
Source noteuspto-grants-2014_12